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肿瘤相关钙信号传导蛋白-2基因对人乳腺癌细胞黏附和侵袭力的影响
引用本文:俞力,詹洪峰,龚丹丹,邱志远,周永静,肖秀娣,武正炎,范钰. 肿瘤相关钙信号传导蛋白-2基因对人乳腺癌细胞黏附和侵袭力的影响[J]. 中华实验外科杂志, 2011, 28(10). DOI: 10.3760/cma.j.issn.1001-9030.2011.10.029
作者姓名:俞力  詹洪峰  龚丹丹  邱志远  周永静  肖秀娣  武正炎  范钰
作者单位:1. 212001,镇江市分子内分泌实验室
2. 江苏大学附属人民医院肿瘤研究所
3. 江苏省人民医院普外科
基金项目:镇江市分子内分泌重点实验室资助项目,江苏省自然科学基金,镇江市社会发展基金
摘    要:目的 观察肿瘤相关钙信号传导蛋白-2(TROP-2)基因小干扰RNA (siRNA)对乳腺癌细胞黏附和侵袭力的影响.方法 培养人乳腺癌Bcap-37、LCC1、MCF-7、MDA-MB-231、MDA-MB-435、MDA-MB-468及ZR75-1细胞株,以荧光实时定量聚合酶链反应(PCR)方法检测TROP-2基因mRNA表达;筛选出TROP-2表达最高者.采用TROP4基因siRNA转染乳腺癌细胞,分别以荧光实时定量RT-PCR和免疫荧光方法观察TROP-2基因mRNA和蛋白水平,然后以噻唑蓝(MTT)比色法检测细胞黏附性,以Transwell方法检测癌细胞侵袭能力.结果 人乳腺癌Bcap-37、LCC1、MCF-7、MDA-MB-231、MDA-MB-35、MDA-MB-468及ZR75-1细胞株TROP-2 mRNA分别是1.362±0.057、2.207±0.056、2.997±0.052、0.136±0.045、0.122±0.025、0.194±0.028和2.706±0.039,以MCF-7细胞最高;以TROP-2 siRNA转染乳腺癌MCF-7细胞后,癌细胞TROP-2基因mRNA和蛋白水平明显下降,且呈浓度依赖性;黏附实验结果显示,5、10、20 nmol/L siRNA组黏附率分别为(52.9±2.5)%、(25.6±2.3)%、(12.8±2.2)%(P<0.01);Transwell实验结果显示,5、10和20 mol/L siRNA组穿过滤膜的细胞分别为78±17、39±15、19±16,而对照组分别为136±25、139±21(P<0.01).结论 TROP-2基因在乳腺癌细胞黏附和侵袭中发挥着重要作用;以siRNA转染乳腺癌细胞,可抑制乳腺癌细胞黏附和侵袭能力.

关 键 词:乳腺癌  肿瘤相关钙信号传导蛋白-2  RNA干扰  侵袭

Effects of TROP-2 gene on adhesion and invasion of human breast cancer cells
YU Li,ZHAN Hong-feng,GONG Dan-dan,QIU Zhi-yuan,ZHOU Yong-jing,XIAO Xiu-di,WU Zheng-yan,FAN Yu. Effects of TROP-2 gene on adhesion and invasion of human breast cancer cells[J]. Chinese Journal of Experimental Surgery, 2011, 28(10). DOI: 10.3760/cma.j.issn.1001-9030.2011.10.029
Authors:YU Li  ZHAN Hong-feng  GONG Dan-dan  QIU Zhi-yuan  ZHOU Yong-jing  XIAO Xiu-di  WU Zheng-yan  FAN Yu
Abstract:Objective To study the effects of tumor-associated calcium signal transducer-2 (TROP-2) gene small interfering RNA (siRNA) on adhesion and invasion of human breast cancer cells.Methods Real time PCR was used to detect the TROP-2 mRNA of seven human breast cancer cell lines:Bcap-37,LCC1,MCF-7,MDA-MB-231,MDA-MB-435,MDA-MB-468,and ZR75-1.The cell line with hifhest TROP-2 expression was transfected with different doses of TROP-2 siRNA.The expression of TROP-2 mRNA and protein was detected by real-time quantitative polymerase chain reaction (PCR) and immumoflurescence method.The cell adhesion was evaluated by methyl thiazol tetrazolium (MTT) assay,and invasion was exmined by boyden chamber,respectively.Results The TROP-2 mRNA in Bcap-37,LCC1,MCF-7,MDA-MB-231,MDA-MB-435,MDA-MB-468 and ZR75-1 cell lines was 1.362 ±0.057,2.207 ± 0.056,2.997 ± 0.052,0.136 ± 0.045,0.122 ± 0.025,0.194 ± 0.028 and 2.706 ± 0.039 respectively,and MCF-7 showed the highest elevation of TROP-2 mRNA.The real-time quantitative PCR and immumoflurescence method revealed that the expression of TROP-2 mRNA and protein was reduced in a time- and dose-dependent manner (P < 0.01 ;P < 0.01 ).The adhesive rate in siRNA groups (5,10 and 20 nmol/L) was (52.9±2.5)%,(25.6±2.3)% and (12.8±2.2)% (P<0.01),respectively.The transwell results showed that the invasion cells were 78 ± 17,39 ± 15,19 ± 16,136 ± 25 and 139 ± 21 in different groups (5,10,20 umol/L siRNA,and controls),respectively (P <0.01 ).Conclusion TROP-2 gene might play an important role in adhesion and invasion of human breast cancer cells.siRNA targeted TROP-2 could effectively inhibit adhesion and invasion of human breast cancer cells.
Keywords:Breast carcinoma  Tumor-associated calcium signal transducer-2  RNA interference  Invasion
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